Canonical Allele Identifier: CA2202047664
Gene: PKD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.2111545C= , CM000678.2:g.2111545C= GRCh38
NC_000016.9:g.2161546C= , CM000678.1:g.2161546C= GRCh37
NC_000016.8:g.2101547C= NCBI36
NG_008617.1:g.29354G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000262304.9:c.3622G= MANE Select ENSP00000262304.4:p.Val1208=
ENST00000262304.8:c.3622G= ENSP00000262304.4:p.Val1208=
ENST00000415938.7:n.310+795G=
ENST00000423118.5:c.3622G= ENSP00000399501.1:p.Val1208=
ENST00000468674.5:n.430+795G=
ENST00000469241.2:n.572G=
ENST00000483024.1:c.233+271G=
ENST00000483731.5:n.790+795G=
ENST00000488185.2:c.473-3187G=
ENST00000565639.6:n.773+795G=
ENST00000568591.5:c.2226+795G= ENSP00000457162.1:n.2226+795G=
ENST00000569983.5:n.421+795G=
NM_000296.3:c.3622G= NP_000287.3:p.Val1208=
NM_001009944.2:c.3622G= NP_001009944.2:p.Val1208=
XM_005255370.2:c.577G= XP_005255427.1:p.Val193=
XM_011522525.1:c.3700G= XP_011520827.1:p.Val1234=
XM_011522526.1:c.3700G= XP_011520828.1:p.Val1234=
XM_011522527.1:c.3700G= XP_011520829.1:p.Val1234=
XM_011522528.1:c.3676G= XP_011520830.1:p.Val1226=
XM_011522529.1:c.3676G= XP_011520831.1:p.Val1226=
XM_011522530.1:c.3646G= XP_011520832.1:p.Val1216=
XM_011522531.1:c.3628G= XP_011520833.1:p.Val1210=
XM_011522532.1:c.3574G= XP_011520834.1:p.Val1192=
XM_011522533.1:c.3493G= XP_011520835.1:p.Val1165=
XM_011522534.1:c.3436G= XP_011520836.1:p.Val1146=
XM_011522535.1:c.1522G= XP_011520837.1:p.Val508=
XM_011522536.1:c.3700G= XP_011520838.1:p.Val1234=
XM_011522537.1:c.700G= XP_011520839.1:p.Val234=
XR_932867.1:n.3715G=
XR_932868.1:n.3715G=
XR_932869.1:n.3715G=
XR_932870.1:n.3715G=
XM_005255370.3:c.577G= XP_005255427.1:p.Val193=
XM_011522528.3:c.3676G= XP_011520830.1:p.Val1226=
XM_011522529.2:c.3676G= XP_011520831.1:p.Val1226=
XM_011522537.2:c.700G= XP_011520839.1:p.Val234=
XM_024450298.1:c.3742G= XP_024306066.1:p.Val1248=
XM_024450299.1:c.3670G= XP_024306067.1:p.Val1224=
XM_024450300.1:c.3532G= XP_024306068.1:p.Val1178=
XM_024450301.1:c.1618G= XP_024306069.1:p.Val540=
NM_000296.4:c.3622G= NP_000287.4:p.Val1208=
NM_001009944.3:c.3622G= MANE Select NP_001009944.3:p.Val1208=